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rs202047589

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs202047589(C;T)
Make rs202047589(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome10
Position97599780
GeneHOGA1
is asnp
is mentioned by
dbSNPrs202047589
ebirs202047589
HLIrs202047589
Exacrs202047589
Varsomers202047589
Maprs202047589
PheGenIrs202047589
hapmaprs202047589
1000 genomesrs202047589
hgdprs202047589
ensemblrs202047589
gopubmedrs202047589
geneviewrs202047589
scholarrs202047589
googlers202047589
pharmgkbrs202047589
gwascentralrs202047589
openSNPrs202047589
23andMers202047589
23andMe allrs202047589
SNP Nexus

SNPshotrs202047589
SNPdbers202047589
MSV3drs202047589
GWAS Ctlgrs202047589
Max Magnitude0
ClinVar
Risk rs202047589(T;T)
Alt rs202047589(T;T)
Reference rs202047589(C;C)
Significance Pathogenic
Disease Primary hyperoxaluria
Variation info
Gene HOGA1
CLNDBN Primary hyperoxaluria, type III
Reversed 0
HGVS NC_000010.10:g.99359537C>T
CLNSRC
CLNACC RCV000186480.1,